OncoRisk Complete is the most extensive, comprehensive oncogenetics panel that covers the analysis of 88 genes to determine the hereditary risks of the most common cancers based on the patient's DNA analysis.
The OncoRisk Complete test examines genetic mutations that can increase the likelihood of developing cancer and provides information about individual risks.
The OncoRisk Complete test will provide accurate and detailed information about the susceptibility to various types of cancer, which will allow early detection of the disease and recommend personalized tests for patients who need treatment with assisted reproductive technologies.
If mutations in genes are detected by the OncoRisk Complete test, a geneticist at IVMED will help you find out important information during a personal consultation at your request.
OncoRisk Complete is an important mechanism for:
For the OncoRisk Complete extended panel of hereditary cancers (88 genes), the material is venous blood or buccal epithelium.
The term for this analysis is 20 working days from the date of receipt of the samples for testing by the laboratory.
Hereditary forms of cancer account for a significant percentage of all cancer cases.
These types of cancer are clearly associated with the inheritance of a gene with a "breakdown" - a pathogenic mutation. Altered genes with mutations are passed down from generation to generation and significantly increase the risk of developing diseases. Each patient carrying a hereditary oncogenic mutation has a several (and sometimes hundreds) times higher chance of contracting a specific cancer.
It is well known that a person inherits 50% of the genes in the germ cells (gametes) from the father and 50% from the mother, meaning that a damaged gene with mutations can be inherited from either parent. The probability of inheriting such a gene is 50%. The same probability of inheriting a mutation exists in the brothers and sisters of a patient who carries mutations in genes. For more distant relatives, the possibility of inheriting mutations decreases in proportion to the degree of kinship.
The following markers indicate a possible hereditary mutation:
If you have a history of cancer in your family, you should find out if you and your family are at risk of developing hereditary forms of cancer.
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By clicking, you accept the terms and conditions “Consent to the collection and processing of personal data” and “Public agreement on the provision of medical services”
